"Xuanjiang" in vitro diagnostic blood bank intelligent decapping centrifuge (unsterilized) - Taiwan Registration 997d412cc1962f0b094dba0b252b23f2
Access comprehensive regulatory information for "Xuanjiang" in vitro diagnostic blood bank intelligent decapping centrifuge (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 997d412cc1962f0b094dba0b252b23f2 and manufactured by LANNER BIOTECHNOLOGY CO., LTD.. The authorized representative in Taiwan is LANNER BIOTECHNOLOGY CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including LANNER BIOTECHNOLOGY CO., LTD., and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Device Details
Product Details
Limited to the classification and grading management method of medical equipment, in vitro diagnostic blood bank centrifuge (B.9275) first level identification range.
B Hematology, pathology, and genetics
B.9275 Blood bank centrifuge for in vitro diagnostics
ๅ็ข;; QMS/QSD
Dates and Status
Oct 01, 2021
Oct 31, 2026